Abstract
Thyrotrophin-releasing factor (TRF) and analogues of its pyroglutamyl ring were tested for their potencies in eliciting thyrotrophin release in vivo. The ratio of potency of an analogue to the potency of TRF was used to predict changes in binding energy of association between the TRF molecule and the TRF-thyrotroph receptor. Assumptions made in this correlation were that the analogue has efficacy and stability to degradation in vivo equal to TRF, and a similar temperature dependence of binding. Types of noncovalent bonds were assigned according to the changes in binding energy. Using the potencies of 23 analogues of TRF in which only the pyroglutamyl residue was modified (some taken from the literature), the following inferences have been drawn about the TRF molecule-TRF-thyrotroph receptor interaction. (a) The ring amide proton is a hydrogen bond acceptor. The strength of this hydrogen bond is approximately 1.5 kcal/ mol. (b) The δ-ketone oxygen is a hydrogen bond donor. The strength of this hydrogen bond is approximately 3.5 kcal/mole. (c) The γ-methylene group is involved in formation of a hydrophobic bond whose strength is approximately 0.8 kcal/mole. (d) The receptor molecule in the region of the ring amide proton cannot accommodate a group larger than a hydrogen atom. (e) There is a tight fit between the receptor and the β- and γ-carbons of the pyroglutamyl ring. (f) The 5-membered ring structure and its puckering are important in maintaining the right spatial location of the ring amide and the δ-ketone. (g) There is room for substitution on the α-carbon of pyroglutamic acid for at least one methyl group. (h) The pyroglutamyl residue may contribute up to 50% of the total binding energy of TRF.
- Copyright © 1977 by Academic Press, Inc.
MolPharm articles become freely available 12 months after publication, and remain freely available for 5 years.Non-open access articles that fall outside this five year window are available only to institutional subscribers and current ASPET members, or through the article purchase feature at the bottom of the page.
|